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dc.contributor.authorde la Serna, Ivana L.
dc.contributor.authorRoy, Kanaklata
dc.contributor.authorCarlson, Kerri A.
dc.contributor.authorImbalzano, Anthony N.
dc.date2022-08-11T08:10:03.000
dc.date.accessioned2022-08-23T16:53:55Z
dc.date.available2022-08-23T16:53:55Z
dc.date.issued2001-08-28
dc.date.submitted2008-08-04
dc.identifier.citationJ Biol Chem. 2001 Nov 2;276(44):41486-91. Epub 2001 Aug 24. <a href="http://dx.doi.org/10.1074/jbc.M107281200">Link to article on publisher's site</a>
dc.identifier.issn0021-9258 (Print)
dc.identifier.doi10.1074/jbc.M107281200
dc.identifier.pmid11522799
dc.identifier.urihttp://hdl.handle.net/20.500.14038/42382
dc.description.abstractCell cycle arrest is critical for muscle differentiation, and the two processes are closely coordinated but temporally separable. SWI/SNF complexes are ATP-dependent chromatin-remodeling enzymes that have been shown to be required for muscle differentiation in cell culture and have also been reported to be required for Rb-mediated cell cycle arrest. We therefore looked more closely at how SWI/SNF enzymes affect the events that occur during MyoD-induced myogenesis, namely, cell cycle regulation and muscle-specific gene expression, in cells that inducibly express dominant negative versions of Brahma (BRM) and Brahma-related gene 1 (BRG1), the ATPase subunits of two distinct SWI/SNF complexes. Although dominant negative BRM and BRG1 inhibited expression of every muscle-specific regulator and structural gene assayed, there was no effect on MyoD-induced activation of cell cycle regulatory proteins, and thus, cells arrested normally. In particular, in the presence or absence of dominant negative BRM or BRG1, MyoD was able to activate expression of p21, cyclin D3, and Rb, all of which are critical for cell cycle withdrawal in the G1/G0 phase of the cell cycle. These findings suggest that at least one basis for the distinct mechanisms that regulate cessation of cell proliferation and muscle-specific gene expression during muscle differentiation is that SWI/SNF-mediated chromatin-remodeling enzymes are required only for the latter.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=11522799&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1074/jbc.M107281200
dc.subjectBase Sequence
dc.subjectCell Cycle
dc.subjectCell Differentiation
dc.subjectCells, Cultured
dc.subjectChromatin
dc.subjectCyclins
dc.subjectDNA Primers
dc.subjectMuscle, Skeletal
dc.subjectMyoD Protein
dc.subjectOncogene Protein p21(ras)
dc.subjectRetinoblastoma Protein
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectTranscription Factors
dc.subjectCell Biology
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleMyoD can induce cell cycle arrest but not muscle differentiation in the presence of dominant negative SWI/SNF chromatin remodeling enzymes
dc.typeJournal Article
dc.source.journaltitleThe Journal of biological chemistry
dc.source.volume276
dc.source.issue44
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/736
dc.identifier.contextkey564651
html.description.abstract<p>Cell cycle arrest is critical for muscle differentiation, and the two processes are closely coordinated but temporally separable. SWI/SNF complexes are ATP-dependent chromatin-remodeling enzymes that have been shown to be required for muscle differentiation in cell culture and have also been reported to be required for Rb-mediated cell cycle arrest. We therefore looked more closely at how SWI/SNF enzymes affect the events that occur during MyoD-induced myogenesis, namely, cell cycle regulation and muscle-specific gene expression, in cells that inducibly express dominant negative versions of Brahma (BRM) and Brahma-related gene 1 (BRG1), the ATPase subunits of two distinct SWI/SNF complexes. Although dominant negative BRM and BRG1 inhibited expression of every muscle-specific regulator and structural gene assayed, there was no effect on MyoD-induced activation of cell cycle regulatory proteins, and thus, cells arrested normally. In particular, in the presence or absence of dominant negative BRM or BRG1, MyoD was able to activate expression of p21, cyclin D3, and Rb, all of which are critical for cell cycle withdrawal in the G1/G0 phase of the cell cycle. These findings suggest that at least one basis for the distinct mechanisms that regulate cessation of cell proliferation and muscle-specific gene expression during muscle differentiation is that SWI/SNF-mediated chromatin-remodeling enzymes are required only for the latter.</p>
dc.identifier.submissionpathoapubs/736
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages41486-91


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